Robotic Mechanical Coring for the Treatment of Moderate to Severe Facial Wrinkles

Launched by VENUS CONCEPT · Oct 12, 2021

Keywords

ClinConnect Summary

This clinical trial is looking at a new treatment for reducing moderate to severe wrinkles on the cheeks using a method called robotic mechanical coring. The goal is to see if this treatment is safe and effective for improving the appearance of wrinkles after two sessions. The study is currently recruiting up to 70 participants, who will be between the ages of 22 and 75 and have a specific level of wrinkles as assessed by a standard scale.

To participate, you should be in good health and not have had certain skin treatments or conditions that could affect the results, like tattoos or recent surgeries in the treatment area. Women who can become pregnant must use reliable birth control during the study. If you choose to join, you can expect to attend follow-up appointments to monitor your progress after the treatments. This trial is an opportunity to help improve wrinkle treatment options while contributing to valuable research.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Male or female subjects between 22 and 75 years of age.
• • 2. Able to read, understand and voluntarily provide written Informed Consent.
• • 3. Able and willing to comply with the treatment/follow-up schedule and requirements.
• • 4. Women of childbearing age are required to be using a reliable method of birth control at least 3 months prior to study enrollment and for the duration of the study and have a negative Urine Pregnancy test at baseline.
• • 5. Fitzpatrick skin type I to IV.
• • 6. Cheek areas are at least a score of 3 using the Lemperle Wrinkle Scale as judged by the Investigator.
• Exclusion Criteria:
• • 1. Previous aesthetic (device and/or surgical) skin treatment (injection of dermal fillers, fat, or botulinum toxin), in the treated areas in the last 6 months.
• • 2. Silicone, Tattoos, body jewelry, that cannot be removed for the duration of treatment and/or any other synthetic material in the treatment area.
• • 3. Any type of scar in the treatment area
• • 4. Excessive sun exposure and use of tanning beds or tanning creams within 30 days to prior to treatment.
• • 5. History of keloid formation or hypertrophic scarring.
• • 6. Active smoker or having quit smoking in the last 3 months.
• • 7. Active, chronic, or recurrent infection including Herpes simplex virus (HSV) infection or history of HSV in the last 6 months.
• • 8. Compromised immune and/or healing system (e.g., poorly controlled diabetes, collagen vascular disease or autoimmune diseases such as scleroderma, morphea, etc.).
• • 9. Hypersensitivity/allergy to analgesic agents, Betadine, tumescent, Tegaderm or tensioning tape that will be used in the study.
• • 10. Co-morbid condition that could limit the ability of the subject to participate in the study or to comply with follow-up requirements.
• • 11. Pregnant, planning pregnancy during the trial course or breastfeeding.
• • 12. History of bleeding disorder or taking medication that can potentially increase bleeding including anticoagulation.
• • 13. Carcinoma, melanoma, or any other cutaneous cancerous condition in the last 6 months.
• • 14. Non-cancerous lesions (e.g. actinic keratosis, vitiligo, cutaneous papules, nodules, active inflammatory lesions) in the region to be treated.
• • 15. Currently or in the last 1-month part of another clinical study of an investigational drug and/or experimental medical device.
• • 16. Any medical condition that, at the discretion of the investigator, would hamper the impact or the healing process and contra-indicate the subject's participation.